Canonical Allele Identifier: CA401791777

Gene: NPC1

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23536745G>T , CM000680.2:g.23536745G>T	GRCh38
NC_000018.9:g.21116709G>T , CM000680.1:g.21116709G>T	GRCh37
NC_000018.8:g.19370707G>T	NCBI36
NG_012795.1:g.54873C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000271.5:c.3173C>A MANE Select	NP_000262.2:p.Ala1058Asp
ENST00000269228.10:c.3173C>A MANE Select	ENSP00000269228.4:p.Ala1058Asp
NM_000271.4:c.3173C>A	NP_000262.2:p.Ala1058Asp
ENST00000269228.9:c.3173C>A	ENSP00000269228.4:p.Ala1058Asp
ENST00000591051.1:c.2251C>A
ENST00000591075.1:n.806C>A
ENST00000591955.1:n.516C>A
XM_005258277.1:c.3224C>A	XP_005258334.1:p.Ala1075Asp
XM_005258278.3:c.3224C>A	XP_005258335.1:p.Ala1075Asp
XM_005258278.5:c.3224C>A	XP_005258335.1:p.Ala1075Asp
XM_005258279.1:c.3173C>A	XP_005258336.1:p.Ala1058Asp
XM_005258279.2:c.3173C>A	XP_005258336.1:p.Ala1058Asp
XM_006722479.2:c.3224C>A	XP_006722542.1:p.Ala1075Asp
XM_006722479.3:c.3224C>A	XP_006722542.1:p.Ala1075Asp
XM_011526015.1:c.2759C>A	XP_011524317.1:p.Ala920Asp
XM_017025784.1:c.3224C>A	XP_016881273.1:p.Ala1075Asp
XM_017025785.1:c.3224C>A	XP_016881274.1:p.Ala1075Asp
XM_017025786.1:c.3173C>A	XP_016881275.1:p.Ala1058Asp
XM_017025787.1:c.3173C>A	XP_016881276.1:p.Ala1058Asp